ENST00000311907.10:c.1285C>T
MANE Select
|
ENSP00000308541.5:p.His429Tyr
|
|
ENST00000311907.9:c.1285C>T
|
ENSP00000308541.5:p.His429Tyr
|
|
ENST00000530231.5:c.1285C>T
|
ENSP00000433907.1:p.His429Tyr
|
|
NM_000506.3:c.1285C>T
|
NP_000497.1:p.His429Tyr
|
|
NM_000506.4:c.1285C>T , LRG_551t1:c.1285C>T
|
NP_000497.1:p.His429Tyr
|
|
NM_001311257.1:c.1237C>T
|
NP_001298186.1:p.His413Tyr
|
|
XR_428840.2:n.1329C>T
|
|
|
XR_428840.4:n.1320C>T
|
|
|
NM_000506.5:c.1285C>T
MANE Select
|
NP_000497.1:p.His429Tyr
|
|
NM_001311257.2:c.1237C>T
|
NP_001298186.1:p.His413Tyr
|
|